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Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization
Fragile X syndrome (FXS) is the most common form of inherited intellectual disability (ID). Anxiety and social withdrawal are considered core features of the FXS phenotype, yet there is limited diagnostic evidence of the prevalence of formal anxiety disorders in FXS. This study assessed the prevalen...
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Formato: | Texto |
Lenguaje: | English |
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Springer US
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3057014/ https://www.ncbi.nlm.nih.gov/pubmed/21475730 http://dx.doi.org/10.1007/s11689-010-9067-y |
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author | Cordeiro, Lisa Ballinger, Elizabeth Hagerman, Randi Hessl, David |
author_facet | Cordeiro, Lisa Ballinger, Elizabeth Hagerman, Randi Hessl, David |
author_sort | Cordeiro, Lisa |
collection | PubMed |
description | Fragile X syndrome (FXS) is the most common form of inherited intellectual disability (ID). Anxiety and social withdrawal are considered core features of the FXS phenotype, yet there is limited diagnostic evidence of the prevalence of formal anxiety disorders in FXS. This study assessed the prevalence of anxiety disorders in a sample of 58 males and 39 females with FXS (ages 5.0–33.3 years). Participants’ parents completed the Anxiety Disorders Interview Schedule (ADIS-IV), a clinical interview based on DSM-IV criteria, and the Anxiety Depression and Mood Scale (ADAMS), a psychiatric disorders screening instrument normed in ID. We conducted cognitive (IQ) and autism (AUT) assessments and surveyed medication use. Despite a high rate of psychopharmacological treatment, 86.2% of males and 76.9% of females met criteria for an anxiety disorder, with social phobia and specific phobia the most commonly diagnosed. Proband status, gender, and IQ were not significantly related to any anxiety disorders, however significantly higher rates of a few anxiety disorders were found in older age and AUT groups. Significant correlations between ADIS diagnoses and ADAMS scores provided cross-validation of instruments, indicating that the ADIS is suitable for use in FXS. A greater percentage of our sample met criteria for most anxiety disorders than has been reported in other ID groups or the general population. The rate of anxiety compared to general ID suggests that the FMR1 full mutation confers an especially high risk for these disorders, regardless of factors commonly associated with FXS clinical involvement. A thorough clinical assessment and treatment of anxiety should be included in the FXS standard of care. |
format | Text |
id | pubmed-3057014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-30570142011-04-05 Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization Cordeiro, Lisa Ballinger, Elizabeth Hagerman, Randi Hessl, David J Neurodev Disord Article Fragile X syndrome (FXS) is the most common form of inherited intellectual disability (ID). Anxiety and social withdrawal are considered core features of the FXS phenotype, yet there is limited diagnostic evidence of the prevalence of formal anxiety disorders in FXS. This study assessed the prevalence of anxiety disorders in a sample of 58 males and 39 females with FXS (ages 5.0–33.3 years). Participants’ parents completed the Anxiety Disorders Interview Schedule (ADIS-IV), a clinical interview based on DSM-IV criteria, and the Anxiety Depression and Mood Scale (ADAMS), a psychiatric disorders screening instrument normed in ID. We conducted cognitive (IQ) and autism (AUT) assessments and surveyed medication use. Despite a high rate of psychopharmacological treatment, 86.2% of males and 76.9% of females met criteria for an anxiety disorder, with social phobia and specific phobia the most commonly diagnosed. Proband status, gender, and IQ were not significantly related to any anxiety disorders, however significantly higher rates of a few anxiety disorders were found in older age and AUT groups. Significant correlations between ADIS diagnoses and ADAMS scores provided cross-validation of instruments, indicating that the ADIS is suitable for use in FXS. A greater percentage of our sample met criteria for most anxiety disorders than has been reported in other ID groups or the general population. The rate of anxiety compared to general ID suggests that the FMR1 full mutation confers an especially high risk for these disorders, regardless of factors commonly associated with FXS clinical involvement. A thorough clinical assessment and treatment of anxiety should be included in the FXS standard of care. Springer US 2010-12-03 /pmc/articles/PMC3057014/ /pubmed/21475730 http://dx.doi.org/10.1007/s11689-010-9067-y Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Article Cordeiro, Lisa Ballinger, Elizabeth Hagerman, Randi Hessl, David Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization |
title | Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization |
title_full | Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization |
title_fullStr | Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization |
title_full_unstemmed | Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization |
title_short | Clinical assessment of DSM-IV anxiety disorders in fragile X syndrome: prevalence and characterization |
title_sort | clinical assessment of dsm-iv anxiety disorders in fragile x syndrome: prevalence and characterization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3057014/ https://www.ncbi.nlm.nih.gov/pubmed/21475730 http://dx.doi.org/10.1007/s11689-010-9067-y |
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